Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74421618-74421772 | Rare:50 | ||||
chr2:74503318-74503484 | Rare:41 | ||||
chr2:74529632-74530036 | Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
chr2:74554621-74554765 | Common:1; Rare:64 | ||||
chr2:74833926-74834137 | Rare:61 | ||||
chr2:74958880-74959071 | Rare:67 | ||||
chr2:84881106-84881228 | Common:1; Rare:28 | ||||
chr2:85354557-85354779 | Common:1; Rare:66 | ||||
chr2:85561441-85561590 | Rare:58; Clinvar:4 | ||||
chr2:85602629-85602895 | Rare:70 | ||||
chr2:85612027-85612173 | Rare:38 | ||||
chr2:86199403-86199487 | Common:1; Rare:29 | ||||
chr2:86563332-86563483 | Common:2; Rare:57 | ||||
chr2:88691441-88691673 | Common:2; Rare:70 | ||||
chr2:95402607-95402797 | Rare:59 |